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【结 构 式】

【分子编号】53106

【品名】6,7-dichloro-5,8-quinolinedione

【CA登记号】n/a

【 分 子 式 】C9H3Cl2NO2

【 分 子 量 】228.03376

【元素组成】C 47.4% H 1.33% Cl 31.09% N 6.14% O 14.03%

与该中间体有关的原料药合成路线共 2 条

合成路线1

该中间体在本合成路线中的序号:(I)

The condensation of 6,7-dichloroquinoline-5,8-dione (I) with 4-(2-aminoethyl)morpholine (II) provided a 2:1 mixture of the title 7-amino quinoline and its 6-amino regioisomer (III), which were separated by column chromatography.

1 Cooley, K.A.; Southwick, E.C.; Ducruet, A.P.; Joo, B.; Vogt, A.; Wipf, P.; Aslan, D.C.; Lazo, J.S.; Discovery and biological evaluation of a new family of potent inhibitors of the dual specificity protein phosphatase Cdc25. J Med Chem 2001, 44, 24, 4042.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 53106 6,7-dichloro-5,8-quinolinedione n/a C9H3Cl2NO2 详情 详情
(II) 12880 4-(2-Aminoethyl)morpholine; 2-(4-Morpholinyl)ethylamine; 2-(4-Morpholinyl)-1-ethanamine; N-(2-Aminoethyl)morpholine; N-Morpholine ethanamide 2038-03-1 C6H14N2O 详情 详情
(III) 53108 7-chloro-6-{[2-(4-morpholinyl)ethyl]amino}-5,8-quinolinedione n/a C15H16ClN3O3 详情 详情

合成路线2

该中间体在本合成路线中的序号:(I)

The condensation of 6,7-dichloroquinoline-5,8-dione (I) with 4-(2-aminoethyl)morpholine (II) provided a 1:2 mixture of the title 6-amino quinoline and its 7-amino regioisomer (III), which were separated by column chromatography.

1 Cooley, K.A.; Southwick, E.C.; Ducruet, A.P.; Joo, B.; Vogt, A.; Wipf, P.; Aslan, D.C.; Lazo, J.S.; Discovery and biological evaluation of a new family of potent inhibitors of the dual specificity protein phosphatase Cdc25. J Med Chem 2001, 44, 24, 4042.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 53106 6,7-dichloro-5,8-quinolinedione n/a C9H3Cl2NO2 详情 详情
(II) 12880 4-(2-Aminoethyl)morpholine; 2-(4-Morpholinyl)ethylamine; 2-(4-Morpholinyl)-1-ethanamine; N-(2-Aminoethyl)morpholine; N-Morpholine ethanamide 2038-03-1 C6H14N2O 详情 详情
(III) 53107 6-chloro-7-{[2-(4-morpholinyl)ethyl]amino}-5,8-quinolinedione n/a C15H16ClN3O3 详情 详情
Extended Information